13C and 1H nuclear magnetic resonance of methyl-substituted acetophenones and methyl benzoates: Steric hindrance and inhibited conjugation

Magnetic Resonance in Chemistry

Volumn 42, Issue 10, 2004, Pages 844-851

  Buděšínský, Miloš ^a   Kulhánek, Jiři ^b   Böhm, Stanislav ^c   Cigler, Petr ^a   Exner, Otto ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b UNIVERSITY OF PARDUBICE   (Czech Republic)

^c INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

Author keywords

13C NMR; 1H NMR; Hindered conjugation; NMR; Steric effect; Substituent effects

Indexed keywords

ATOMS; KETONES; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

13C NMR; 1H NMR; ACETOPHENONES; B3LYP/6-311++G; C ATOMS; HINDERED CONJUGATION; METHYL BENZOATE; STERIC EFFECT; SUBSTITUENT EFFECT; ZERO VALUES;

CONFORMATIONS;

2,6 DIMETHYLACETOPHENONE; ACETOPHENONE DERIVATIVE; BENZOIC ACID DERIVATIVE; CARBON 13; FUNCTIONAL GROUP; METHYL GROUP; PROTON; UNCLASSIFIED DRUG; CARBON; HYDROGEN; METHYL BENZOATE;

ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; CONFORMATION; CORRELATION ANALYSIS; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION; CHEMISTRY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ACETOPHENONES; BENZOATES; CARBON ISOTOPES; HYDROGEN; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION;

EID: 10944224532     PISSN: 07491581     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrc.1414     Document Type: Article

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